chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	44739048	44739049	T	A	32	GENIC	homozygous	117008340
10	44740023	44740024	G	A	24	GENIC	homozygous	116930542
10	44740256	44740257	T	C	33	GENIC	possibly homozygous	116771053
10	44740275	44740276	T	C	30	GENIC	homozygous	116930544
10	44740826	44740827	T	C	17	GENIC	homozygous	116771055
10	44740995	44740996	A	C	26	GENIC	homozygous	116771057
10	44742069	44742070	T	C	23	GENIC	homozygous	116771059
10	44742124	44742125	C	T	22	GENIC	homozygous	116771061
10	44742825	44742826	A	G	140	GENIC	heterozygous	117992862
10	44742845	44742846	G	A	144	GENIC	heterozygous	118066384
10	44743116	44743117	A	G	42	GENIC	heterozygous	118066385
10	44743175	44743176	A	G	58	GENIC	heterozygous	118066386
10	44743250	44743251	G	A	16	GENIC	heterozygous	118066387
10	44744028	44744029	G	A	18	GENIC	homozygous	116771063
10	44744718	44744719	A	G	31	GENIC	homozygous	116771065
10	44744730	44744731	G	T	27	GENIC	homozygous	116771067
10	44744760	44744761	G	A	21	GENIC	homozygous	116771069
10	44744909	44744910	G	A	25	GENIC	homozygous	116771071
10	44745343	44745344	C	G	17	GENIC	heterozygous	118066390
10	44745459	44745460	G	A	20	GENIC	homozygous	116771073
10	44745916	44745917	G	A	19	GENIC	homozygous	116771075
10	44746527	44746528	G	T	35	GENIC	homozygous	116771077
10	44746602	44746603	T	C	34	GENIC	homozygous	116930550
10	44746870	44746871	T	G	31	GENIC	homozygous	116771079
10	44745355	44745356	G	C	22	GENIC	heterozygous	118074655